D J Abraham

发表

QSAR: Hydropathic analysis of inhibitors of the p53–mdm2 interaction

D. Abraham, P S Galatin, D J Abraham, 2001, Proteins.

Computational methodology for estimating changes in free energies of biomolecular association upon mutation. The importance of bound water in dimer-tetramer assembly for beta 37 mutant hemoglobins.

G E Kellogg, D. Abraham, G. Kellogg, 2000, Biochemistry.

Computationally accessible method for estimating free energy changes resulting from site‐specific mutations of biomolecules: Systematic model building and structural/hydropathic analysis of deoxy and oxy hemoglobins

G E Kellogg, D. Abraham, G. Kellogg, 2001, Proteins.

Structure of human erythrocyte catalase.

Changqing, D. Abraham, T. Ko, 2000, Acta crystallographica. Section D, Biological crystallography.

Hydrophobicity: is LogP(o/w) more than the sum of its parts?

D. Abraham, D J Abraham, G Eugene Kellogg, 2000, European journal of medicinal chemistry.

The enigma of the liganded hemoglobin end state: a novel quaternary structure of human carbonmonoxy hemoglobin.

D. Abraham, M. Safo, D J Abraham, 2005, Biochemistry.

Extension of the fragment method to calculate amino acid zwitterion and side chain partition coefficients

A. Leo, D. Abraham, D J Abraham, 1987, Proteins.

Hydropathic analysis of the non-covalent interactions between molecular subunits of structurally characterized hemoglobins.

G E Kellogg, G. K. Ackers, D. Abraham, 1997, Journal of molecular biology.

Allosteric modifiers of hemoglobin. 2. Crystallographically determined binding sites and hydrophobic binding/interaction analysis of novel hemoglobin oxygen effectors.

G E Kellogg, D. Abraham, G. Kellogg, 1991, Journal of medicinal chemistry.

KEY, LOCK, and LOCKSMITH: complementary hydropathic map predictions of drug structure from a known receptor-receptor structure from known drugs.

G E Kellogg, D. Abraham, G. Kellogg, 1992, Journal of molecular graphics.